Lake Region Mfg., Inc.
HYDROPHILIC GUIDEWIRE
SKU K033758UPC DQX
In Stock
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IIFDA 510(k) Cleared (K033758)
1
Free shipping on orders over $99 · 30-day returns
Lake Region Mfg., Inc.
Free shipping on orders over $99 · 30-day returns
HYDROPHILIC GUIDEWIRE is an FDA 510(k)-cleared medical device (K033758) manufactured by Lake Region Mfg., Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 18, 2003. Regulation: 8.
